Canonical Allele Identifier: CA7630587

Gene: CLN6

Linked Data

• dbSNP Id: rs749797436
• ExAC: 15:68503947 T / G
• gnomAD v2: 15-68503947-T-G
• gnomAD v4: 15-68211609-T-G
• MyVariant Identifiers: chr15:g.68503947T>G (hg19) ; chr15:g.68211609T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211609T>G , CM000677.2:g.68211609T>G	GRCh38
NC_000015.9:g.68503947T>G , CM000677.1:g.68503947T>G	GRCh37
NC_000015.8:g.66291001T>G	NCBI36
NG_008764.2:g.50603A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+66A>C MANE Select	ENSP00000249806.5:n.486+66A>C
ENST00000562767.2:c.84-13981A>C	ENSP00000456336.1:n.84-13981A>C
ENST00000563917.2:n.328+66A>C
ENST00000565471.6:c.84-1850A>C	ENSP00000457384.1:n.84-1850A>C
ENST00000635747.1:c.*389+66A>C	ENSP00000490627.1:n.*389+66A>C
ENST00000636212.1:c.*103A>C	ENSP00000489851.1:n.*103A>C
ENST00000636314.1:c.183-291A>C	ENSP00000490295.1:n.183-291A>C
ENST00000636674.1:n.1535A>C
ENST00000636964.1:n.1724A>C
ENST00000637054.1:c.198+6927A>C	ENSP00000490807.1:n.198+6927A>C
ENST00000637223.1:c.*201-291A>C	ENSP00000490010.1:n.*201-291A>C
ENST00000637329.1:c.455+66A>C
ENST00000637450.1:c.*140+66A>C	ENSP00000490204.1:n.*140+66A>C
ENST00000637494.1:c.199-291A>C	ENSP00000490057.1:n.199-291A>C
ENST00000637667.1:c.387+66A>C	ENSP00000489843.1:n.387+66A>C
ENST00000637823.1:c.258A>C
ENST00000637888.1:c.198+6927A>C	ENSP00000490546.1:n.198+6927A>C
ENST00000638076.1:c.*36A>C	ENSP00000490373.1:n.*36A>C
ENST00000638144.1:n.130-291A>C
ENST00000646164.1:c.38+6927A>C
ENST00000249806.9:c.486+66A>C	ENSP00000249806.5:n.486+66A>C
ENST00000538696.5:c.582+66A>C	ENSP00000445770.1:n.582+66A>C
ENST00000562767.1:c.84-13981A>C	ENSP00000456336.1:n.84-13981A>C
ENST00000563917.1:n.333A>C
ENST00000564752.1:c.512+40A>C	ENSP00000457822.1:n.512+40A>C
ENST00000565471.5:c.84-1850A>C	ENSP00000457384.1:n.84-1850A>C
ENST00000566347.5:c.298-291A>C	ENSP00000457783.1:n.298-291A>C
ENST00000567060.5:c.298-1889A>C	ENSP00000454818.1:n.298-1889A>C
NM_017882.2:c.486+66A>C	NP_060352.1:n.486+66A>C
XR_931861.1:n.655A>C
NM_017882.3:c.486+66A>C MANE Select	NP_060352.1:n.486+66A>C